Run ID: ERR2229791
Sample name:
Date: 31-03-2023 17:35:37
Number of reads: 16564
Percentage reads mapped: 22.14
Strain: lineage4.9
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.67 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.55 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.83 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8264 | c.963T>C | synonymous_variant | 1.0 |
gyrA | 8267 | c.966G>C | synonymous_variant | 1.0 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.4 |
gyrA | 8316 | p.Thr339Glu | missense_variant | 0.4 |
gyrA | 8320 | p.Ser340Asn | missense_variant | 0.4 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.4 |
gyrA | 8325 | p.Gly342Ser | missense_variant | 0.4 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.4 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.4 |
gyrA | 8354 | c.1053G>C | synonymous_variant | 0.4 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.8 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.8 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.8 |
rpoB | 761064 | p.Ala420Ser | missense_variant | 0.8 |
rpoB | 761084 | c.1278C>G | synonymous_variant | 0.4 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.4 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.4 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.4 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.67 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.67 |
rpoB | 761974 | p.His723Leu | missense_variant | 0.8 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.8 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.8 |
rpoB | 762009 | p.Leu735Met | missense_variant | 0.8 |
rpoB | 762015 | p.Glu737Ser | missense_variant | 0.8 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.8 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.8 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.8 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.8 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.8 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 1.0 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 1.0 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 1.0 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 1.0 |
rpoB | 762870 | p.Met1022Gln | missense_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.89 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.88 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.88 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.88 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.83 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.75 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.75 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.75 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.75 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.75 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.75 |
rpoB | 763050 | p.Leu1082Met | missense_variant | 1.0 |
rpoC | 763501 | p.Asp44Glu | missense_variant | 1.0 |
rpoC | 763504 | c.135C>T | synonymous_variant | 1.0 |
rpoC | 763511 | p.Cys48Asp | missense_variant | 1.0 |
rpoC | 763517 | p.Lys50Arg | missense_variant | 1.0 |
rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.83 |
rpoC | 763621 | c.252C>G | synonymous_variant | 0.88 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.83 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.86 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.83 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.8 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.75 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.75 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.75 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.83 |
rpoC | 764527 | c.1158C>G | synonymous_variant | 0.83 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.71 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.75 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.78 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.67 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.67 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.67 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.67 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.67 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.57 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.57 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.71 |
rpoC | 764621 | c.1252_1254delCTCinsTTG | synonymous_variant | 0.71 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.71 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.71 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 1.0 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 1.0 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
rpoC | 764681 | p.Leu438Met | missense_variant | 1.0 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 1.0 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 1.0 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 1.0 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 1.0 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
rpoC | 764804 | p.Gln479Phe | missense_variant | 1.0 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 1.0 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 1.0 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 1.0 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 1.0 |
rpoC | 764837 | p.Val490Ile | missense_variant | 1.0 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 1.0 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
rpoC | 764863 | c.1494G>C | synonymous_variant | 1.0 |
rpoC | 764872 | c.1503A>C | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.67 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.67 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.67 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.4 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.4 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.4 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.5 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.5 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.5 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.5 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472224 | n.379G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472674 | n.829T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474284 | n.631_633delCCT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474293 | n.637_651delCCTCTCCGGAGGAGG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474355 | n.698A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474384 | n.727C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474406 | n.749T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474496 | n.839C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474633 | n.977_981delTCACC | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474640 | n.983_984insTTGCT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474658 | n.1001A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474675 | n.1018C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474691 | n.1034A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060_1061insGTTTT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474836 | n.1179A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475515 | n.1858G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112_2113insC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476519 | n.2862C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476530 | n.2873C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476534 | n.2877A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 1.0 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 1.0 |
rpsA | 1834285 | c.744G>C | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 1.0 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 1.0 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 1.0 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 1.0 |
clpC1 | 4038563 | c.2142C>T | synonymous_variant | 1.0 |
clpC1 | 4038566 | p.Ile713Val | missense_variant | 1.0 |
clpC1 | 4038596 | p.Lys703Glu | missense_variant | 1.0 |
clpC1 | 4038602 | c.2103G>C | synonymous_variant | 1.0 |
clpC1 | 4039886 | c.819C>G | synonymous_variant | 1.0 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
clpC1 | 4039916 | c.789T>G | synonymous_variant | 1.0 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |